Canonical Allele Identifier: CA7041166

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs756544326
• ExAC: 13:103508371 T / A
• gnomAD v2: 13-103508371-T-A
• gnomAD v3: 13-102856021-T-A
• gnomAD v4: 13-102856021-T-A
• MyVariant Identifiers: chr13:g.103508371T>A (hg19) ; chr13:g.102856021T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102856021T>A , CM000675.2:g.102856021T>A	GRCh38
NC_000013.10:g.103508371T>A , CM000675.1:g.103508371T>A	GRCh37
NC_000013.9:g.102306372T>A	NCBI36
NG_007146.1:g.15198T>A , LRG_464:g.15198T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682632.1:n.709-31T>A (ERCC5)
ENST00000682869.1:n.1117-31T>A (ERCC5)
ENST00000683246.1:n.1245-31T>A (ERCC5)
ENST00000684184.1:n.1114-31T>A (ERCC5)
ENST00000638434.1:c.566-31T>A (BIVM-ERCC5)
ENST00000639132.1:c.1143-31T>A (BIVM-ERCC5)	ENSP00000492684.1:n.1143-31T>A
ENST00000639435.1:c.1830-31T>A (BIVM-ERCC5)	ENSP00000491742.1:n.1830-31T>A
ENST00000651002.1:c.*229-31T>A (ERCC5)	ENSP00000498809.1:n.*229-31T>A
ENST00000651055.1:n.597-31T>A (ERCC5)
ENST00000651281.1:n.836-31T>A (ERCC5)
ENST00000651470.1:c.468-31T>A (ERCC5)	ENSP00000498701.1:n.468-31T>A
ENST00000652225.2:c.468-31T>A (ERCC5) MANE Select	ENSP00000498881.2:n.468-31T>A
ENST00000652613.1:c.-37-31T>A (ERCC5)	ENSP00000498357.1:n.-37-31T>A
ENST00000355739.8:c.468-31T>A (ERCC5)	ENSP00000347978.4:n.468-31T>A
ENST00000535557.5:c.468-31T>A (ERCC5)	ENSP00000442117.1:n.468-31T>A
ENST00000602836.1:c.1744-31T>A (BIVM-ERCC5)
ENST00000610537.4:c.468-31T>A (ERCC5)	ENSP00000478667.1:n.468-31T>A
NM_000123.3:c.468-31T>A , LRG_464t1:c.468-31T>A (ERCC5)	NP_000114.2:n.468-31T>A
NM_001204425.1:c.1830-31T>A (BIVM-ERCC5)	NP_001191354.1:n.1830-31T>A
NM_000123.4:c.468-31T>A (ERCC5) MANE Select	NP_000114.3:n.468-31T>A
NM_001204425.2:c.1830-31T>A (BIVM-ERCC5)	NP_001191354.2:n.1830-31T>A